Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference27 articles.
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2. Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome;Belloso;European Journal of Human Genetics,2007
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1. Mitochondrial tRNA mutations in Chinese children with tic disorders;Bioscience Reports;2020-12
2. Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion;Behavioral and Brain Functions;2018-02-20
3. Functional Evaluations of Genes Disrupted in Patients with Tourette’s Disorder;Frontiers in Psychiatry;2016-02-09
4. Genetics of Mitochondrial Disease with Focus on Movement Disorders;Movement Disorder Genetics;2015
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